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EGFR tyrosine kinase inhibitors versus chemotherapy as first-line therapy for non-small cell lung cancer patients with the L858R point mutation

机译:EGFR酪氨酸激酶抑制剂与化学疗法作为L858R点突变的非小细胞肺癌患者的一线治疗

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摘要

The efficacy of EGFR tyrosine kinase inhibitors (TKIs) varies among different EGFR mutations. Here, we directly compared the efficacy of first-line TKIs to chemotherapy for non-small cell lung cancer (NSCLC) patients with the L858R mutation. The progression-free survival (PFS) for patients receiving TKIs as first-line therapy was longer than those who received chemotherapy (hazard ratio [HR]: 0.44, P < 0.001). Subgroup analyses showed that first-line TKI therapy resulted in longer PFS among non-smokers (HR: 0.41, P < 0.001), male (HR: 0.49, P = 0.002), female (HR: 0.39, P < 0.001), and patients with adenocarcinoma histology (HR: 0.41, P < 0.001). However, among patients with non-adenocarcinoma histology (HR: 1.11, P = 0.824) and those who used to smoke (HR: 0.55, P = 0.093), first-line TKI therapy failed to demonstrate statistically longer PFS compared to chemotherapy. Our results demonstrated that for patients with L858R mutation, first-line TKI therapy provided better survival benefits. However, among non-adenocarcinoma patients and those who used to smoke, the PFS in cohorts receiving first-line chemotherapy or TKI were not significantly different. The results of the current study will be helpful for decision-making in the treatment of patients with L858R mutation.
机译:EGFR酪氨酸激酶抑制剂(TKI)的功效因不同的EGFR突变而异。在这里,我们直接比较了一线TKI与具有L858R突变的非小细胞肺癌(NSCLC)患者化疗的疗效。接受TKIs作为一线治疗的患者的无进展生存期(PFS)长于接受化疗的患者(危险比[HR]:0.44,P <0.001)。亚组分析显示,一线TKI治疗可导致非吸烟者(HR:0.41,P <0.001),男性(HR:0.49,P = 0.002),女性(HR:0.39,P <0.001)和更长的PFS更长。腺癌组织学患者(HR:0.41,P 0.001)。然而,在非腺癌组织学(HR:1.11,P = 0.824)和曾经吸烟的患者(HR:0.55,P = 0.093)中,与化疗相比,一线TKI治疗未能显示出统计学上更长的PFS。我们的结果表明,对于L858R突变的患者,一线TKI治疗可提供更好的生存获益。但是,在非腺癌患者和曾经吸烟的患者中,接受一线化疗或TKI的队列中的PFS没有显着差异。本研究的结果将有助于L858R突变患者的治疗决策。

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